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Acute Myeloid Leukemia (AML) and Related Precursor Neoplasms
- AML with Recurrent Genetic Abnormalities
- AML with Myelodysplasia-Related Changes
- sub division
- sub-sub-sub division
- sub division
Acute Myeloid Leukemia (AML) and Related Precursor Neoplasms
- AML with t(8;21)(q22;q22.1); RUNX1-RUNX1T1 - AML with with inv(16)(p13.1q22) or t(16;16)(p13.1;q22); CBFB-MYH11 - Acute Promyelocytic Leukemia (APL) with PML-RARA - AML with t(9;11)(p21.3;q23.3); KMT2A-MLLT3 - AML with t(6;9)(p23;q34.1); DEK-NUP214 - AML with inv(3)(q21.3q26.2) or t(3;3)(q21.3;q26.2);GATA2, MECOM - AML Megakaryoblastic with t(1;22)(p13.3;q13.1);RBM15-MKL1 - AML with BCR-ABL1 - AML with Mutated NPM1 - AML with Biallelic Mutations of CEBPA - AML with Mutated RUNX1
- AML with Minimal Differentiation - AML without Maturation - AML with Maturation - Acute Myelomonocytic Leukemia - Acute Monoblastic and Monocytic Leukemia - Pure Erythroid Leukemia - Acute Megakaryoblastic Leukemia (AMKL) - Acute Basophilic Leukemia - Acute Panmyelosis with Myelofibrosis
- Transient Abnormal Myelopoiesis (TAM) Associated with Down Syndrome - Myeloid Leukemia Associated with Down Syndrome
- Acute Undifferentiated Leukemia - Mixed Phenotype Acute Leukemia (MPAL) with t(9;22)(q34.1;q11.2); BCR-ABL1 - Mixed Phenotype Acute Leukemia (MPAL) with t(v;11q23.3); KMT2A Rearranged - Mixed Phenotype Acute Leukemia (MPAL), B/Myeloid, Not Otherwise Specified - Mixed Phenotype Acute Leukemia (MPAL), T/Myeloid, Not Otherwise Specified - Mixed-Phenotype Acute Leukemia, Not Otherwise Specified (NOS), Rare Types - Acute Leukemias of Ambiguous Lineage, Not Otherwise Specified (NOS)
- Acute Myeloid Leukaemia with Germline CEBPA Mutation - Myeloid Neoplasms with Germline DDX41 Mutation - Myeloid Neoplasms with Germline RUNX1 Mutation - Myeloid Neoplasms with Germline ANKRD26 Mutation - Myeloid Neoplasms with Germline ETV6 Mutation - Myeloid Neoplasms with Germline GATA2 Mutation
Myelodysplastic Syndromes (MDS)
- MDS with Single Lineage Dysplasia
- MDS with Ring Sideroblasts (MDS-RS)
- MDS with Ring Sideroblasts and Multilineage Dysplasia
- MDS with Multilineage Dysplasia
- MDS with Excess Blasts
- MSD with Isolated del(5q)
- MDS, Unclassifiable
- Refractory Cytopenia of Childhood
Myeloproliferative Neoplasms (MPN)
- Chronic Myeloid Leukemia (CML), BCR-ABL1 Positive
- Chronic Neutrophilic Leukemia (CNL)
- Polycythemia Vera (PV)
- Primary Myelofibrosis (PMF)
- Essential Thrombocythemia (ET)
- Chronic Eosinophilic Leukemia, Not Otherwise Specified
- Myeloproliferative Neoplasm (MPN), Unclassifiable
Myelodysplastic/Myeloproliferative Neoplasms (MDS/MPN)
- Chronic Myelomonocytic Leukemia (CMML)
- Atypical Chronic Myeloid Leukemia (aCML), BCR-ABL1 Negative
- Juvenile Myelomonocytic Leukemia (JMML)
- MDS/MPN with Ring Sideroblasts and Thrombocytosis (MDS/MPN-RS-T)
- MDS/MPN, Unclassifiable
Mature B-Cell Neoplasms
- Monoclonal B-cell Lymphocytosis
- Splenic Diffuse Red Pulp Small B-cell Lymphoma - Hairy Cell Leukemia Variant
- Waldenstrom Macroglobulinemia
- Mu Heavy Chain Disease - Gamma Heavy Chain Disease - Alpha Heavy Chain Disease
- Non-IgM Monoclonal Gammopathy of Undetermined Significance - Plasma Cell Myeloma - Plasma Cell Myeloma Variants - Plasmacytoma - Monoclonal Immunoglobulin Deposition Diseases - Primary Amyloidosis - Light Chain and Heavy Chain Deposition Disease - Plasma Cell Neoplasms with Associated Paraneoplastic Syndrome - POEMS Syndrome - TEMPI Syndrome
- Paediatric Nodal Marginal Zone Lymphoma
- Testicular Follicular Lymphoma - In Situ Follicular Neoplasia - Duodenal-Type Follicular Lymphoma
- Leukemic Non-Nodal Mantle Cell Lymphoma - In Situ Mantle Cell Neoplasia
- Fibrin-Associated Diffuse Large B-cell Lymphoma
- Multicentric Castleman Disease - HHV8-Positive Diffuse Large B-cell Lymphoma, Not Otherwise Specified (NOS) - HHV8-Positive Germinotropic Lymphoproliferative Disorder
- High-Grade B-cell Lymphoma with MYC and BCL2 and/or BCL6 Rearrangements - High-Grade B-cell Lymphoma, Not Otherwise Specified (NOS)
Mature T- and NK-cell Neoplasms
- Systemic EBV-Positive T-cell Lymphoma of Childhood - Chronic Active EBV Infection of T- and NK-cell Type, Systemic Form - Hydroa Vacciniforme-Like Lymphoproliferative Disorder - Severe Mosquito Bite Allergy
- Enteropathy-Associated T-cell Lymphoma - Monomorphic Epitheliotropic Intestinal T-cell Lymphoma - Intestinal T-cell Lymphoma, Not Otherwise Specified (NOS) - Indolent T-cell Lymphoproliferative Disorder of the Gastrointestinal Tract
- Lymphomatoid Papulosis - Primary Cutaneous Anaplastic Large Cell Lymphoma
- Primary Cutaneous Gamma Delta T-cell Lymphoma - Primary Cutaneous CD8+ Aggressive Epidermotropic Cytotoxic T-cell Lymphoma - Primary Cutaneous Acral CD8+ T-cell Lymphoma - Primary Cutaneous CD4+ Small/Medium T-cell Lymphoproliferative Disorder
- Angioimmunoblastic T-cell Lymphoma - Follicular T-cell Lymphoma - Nodal Peripheral T-cell Lymphoma with T Follicular Helper Phenotype
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